A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610376



Internal ID20983447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124955186..124955678hg38UCSC Ensembl
chr6:125276332..125276824hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139564
Samples
Known GenesSTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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